ID: ALA292775

Max Phase: Preclinical

Molecular Formula: C18H14ClNO3

Molecular Weight: 327.77

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(NCc1ccc(Cl)cc1)c1cc2cccc(O)c2cc1O

Standard InChI:  InChI=1S/C18H14ClNO3/c19-13-6-4-11(5-7-13)10-20-18(23)15-8-12-2-1-3-16(21)14(12)9-17(15)22/h1-9,21-22H,10H2,(H,20,23)

Standard InChI Key:  GWKYLSPGXDVNHO-UHFFFAOYSA-N

Associated Targets(Human)

DNA polymerase alpha subunit 225 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HFF 3142 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human herpesvirus 6 DNA polymerase 36 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 327.77Molecular Weight (Monoisotopic): 327.0662AlogP: 3.83#Rotatable Bonds: 3
Polar Surface Area: 69.56Molecular Species: NEUTRALHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.83CX Basic pKa: CX LogP: 4.41CX LogD: 4.27
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.68Np Likeness Score: -0.76

References

1. Vaillancourt VA, Cudahy MM, Staley SA, Brideau RJ, Conrad SJ, Knechtel ML, Oien NL, Wieber JL, Yagi Y, Wathen MW..  (2000)  Naphthalene carboxamides as inhibitors of human cytomegalovirus DNA polymerase.,  10  (18): [PMID:10999475] [10.1016/s0960-894x(00)00402-9]

Source